Novel homozygous deletion of segmental KAL1 and entire STS cause Kallmann syndrome and X‐linked ichthyosis in a Chinese family

Publisher： John Wiley & Sons Inc

E-ISSN： 1439-0272|47|10|1160-1165

ISSN： 0303-4569

Source： ANDROLOGIA (ELECTRONIC), Vol.47, Iss.10, 2015-12, pp. : 1160-1165

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